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Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens

Photobiomodulation (PBM) utilises light energy to treat oral disease, periodontitis. However, there remains inconsistency in the reporting of treatment parameters and a lack of knowledge as to how PBM elicits its molecular effects in vitro. Therefore, this study aimed to establish the potential immu...

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Autores principales: Serrage, H. J., Cooper, P. R., Palin, W. M., Horstman, P., Hadis, M., Milward, M. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593050/
https://www.ncbi.nlm.nih.gov/pubmed/33991267
http://dx.doi.org/10.1007/s10103-021-03331-z
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author Serrage, H. J.
Cooper, P. R.
Palin, W. M.
Horstman, P.
Hadis, M.
Milward, M. R.
author_facet Serrage, H. J.
Cooper, P. R.
Palin, W. M.
Horstman, P.
Hadis, M.
Milward, M. R.
author_sort Serrage, H. J.
collection PubMed
description Photobiomodulation (PBM) utilises light energy to treat oral disease, periodontitis. However, there remains inconsistency in the reporting of treatment parameters and a lack of knowledge as to how PBM elicits its molecular effects in vitro. Therefore, this study aimed to establish the potential immunomodulatory effects of blue and near infra-red light irradiation on gingival fibroblasts (GFs), a key cell involved in the pathogenesis of periodontitis. GFs were seeded in 96-well plates in media + / − Escherichia coli lipopolysaccharide (LPS 1 μg/ml), or heat-killed Fusobacterium nucleatum (F. nucleatum, 100:1MOI) or Porphyromonas gingivalis (P. gingivalis, 500:1MOI). Cultures were incubated overnight and subsequently irradiated using a bespoke radiometrically calibrated LED array (400–830 nm, irradiance: 24 mW/cm(2) dose: 5.76 J/cm(2)). Effects of PBM on mitochondrial activity (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and adenosine triphosphate (ATP) assays, total reactive oxygen species production (ROS assay) and pro-inflammatory/cytokine response (interleukin-8 (IL-8) and tumour growth factor-β1 (TGFβ1)) were assessed 24 h post-irradiation. Data were analysed using one-way ANOVA followed by the Tukey test. Irradiation of untreated (no inflammatory stimulus) cultures at 400 nm induced 15%, 27% and 13% increases in MTT, ROS and IL-8 levels, respectively (p < 0.05). Exposure with 450 nm light following application of P. gingivalis, F. nucleatum or LPS induced significant decreases in TGFβ1 secretion relative to their bacterially stimulated controls (p < 0.001). Following stimulation with P. gingivalis, 400 nm irradiation induced 14% increases in MTT, respectively, relative to bacteria-stimulated controls (p < 0.05). These findings could identify important irradiation parameters to enable management of the hyper-inflammatory response characteristic of periodontitis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10103-021-03331-z.
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spelling pubmed-85930502021-11-19 Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens Serrage, H. J. Cooper, P. R. Palin, W. M. Horstman, P. Hadis, M. Milward, M. R. Lasers Med Sci Original Article Photobiomodulation (PBM) utilises light energy to treat oral disease, periodontitis. However, there remains inconsistency in the reporting of treatment parameters and a lack of knowledge as to how PBM elicits its molecular effects in vitro. Therefore, this study aimed to establish the potential immunomodulatory effects of blue and near infra-red light irradiation on gingival fibroblasts (GFs), a key cell involved in the pathogenesis of periodontitis. GFs were seeded in 96-well plates in media + / − Escherichia coli lipopolysaccharide (LPS 1 μg/ml), or heat-killed Fusobacterium nucleatum (F. nucleatum, 100:1MOI) or Porphyromonas gingivalis (P. gingivalis, 500:1MOI). Cultures were incubated overnight and subsequently irradiated using a bespoke radiometrically calibrated LED array (400–830 nm, irradiance: 24 mW/cm(2) dose: 5.76 J/cm(2)). Effects of PBM on mitochondrial activity (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and adenosine triphosphate (ATP) assays, total reactive oxygen species production (ROS assay) and pro-inflammatory/cytokine response (interleukin-8 (IL-8) and tumour growth factor-β1 (TGFβ1)) were assessed 24 h post-irradiation. Data were analysed using one-way ANOVA followed by the Tukey test. Irradiation of untreated (no inflammatory stimulus) cultures at 400 nm induced 15%, 27% and 13% increases in MTT, ROS and IL-8 levels, respectively (p < 0.05). Exposure with 450 nm light following application of P. gingivalis, F. nucleatum or LPS induced significant decreases in TGFβ1 secretion relative to their bacterially stimulated controls (p < 0.001). Following stimulation with P. gingivalis, 400 nm irradiation induced 14% increases in MTT, respectively, relative to bacteria-stimulated controls (p < 0.05). These findings could identify important irradiation parameters to enable management of the hyper-inflammatory response characteristic of periodontitis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10103-021-03331-z. Springer London 2021-05-15 2021 /pmc/articles/PMC8593050/ /pubmed/33991267 http://dx.doi.org/10.1007/s10103-021-03331-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Serrage, H. J.
Cooper, P. R.
Palin, W. M.
Horstman, P.
Hadis, M.
Milward, M. R.
Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title_full Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title_fullStr Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title_full_unstemmed Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title_short Photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
title_sort photobiomodulation of oral fibroblasts stimulated with periodontal pathogens
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593050/
https://www.ncbi.nlm.nih.gov/pubmed/33991267
http://dx.doi.org/10.1007/s10103-021-03331-z
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